---
title: "NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I — FDA record Z-0028-2026 | Is It on Recall"
description: "Fluctuations may be more likely to occur if the total flow through the device sensor (used by the device to determine flow) is less than the minimum device requ"
url: https://isitonrecall.com/recall/fda-device-z-0028-2026-noxboxi-nitric-oxide-delivery-system-model-numbers-noxbox-i/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I — FDA record Z-0028-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 9, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
- **Reason**: Fluctuations may be more likely to occur if the total flow through the device sensor (used by the device to determine flow) is less than the minimum device requirement of 0.5 LPM. In addition, dose fluctuations have been observed when Bunnel LifePulse HFJV system or conventional ventilators have the following device settings: low service pressures generally less than 3.0 PSI, a pressure difference greater than 5.0cm H2O; or at breath per minute rates of 300 (5 Hz).
- **Classification**: Class I
- **Recalling firm**: NOXBOX LTD
- **Quantity**: 1667 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0028-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0028-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model Numbers: (1) NOXBOXI (NBL (Manufacturer)), (2) REQNOXBOXI (Linde (U.S. Distributor)); UDI-DI: 05060541640009; All serial numbers. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic: TN

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Tennessee](https://isitonrecall.com/state/tennessee/)

## Dates in the source

- **Report date**: Oct 15, 2025
- **Recall initiation date**: Sep 9, 2025
- **Center classification date**: Oct 6, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0028-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [NOXBOX LTD records](https://isitonrecall.com/brand/noxbox-ltd/)